JPH0476363B2 - - Google Patents
Info
- Publication number
- JPH0476363B2 JPH0476363B2 JP60284285A JP28428585A JPH0476363B2 JP H0476363 B2 JPH0476363 B2 JP H0476363B2 JP 60284285 A JP60284285 A JP 60284285A JP 28428585 A JP28428585 A JP 28428585A JP H0476363 B2 JPH0476363 B2 JP H0476363B2
- Authority
- JP
- Japan
- Prior art keywords
- meth
- acrylate
- propane
- general formula
- bis
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000178 monomer Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 19
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 230000009974 thixotropic effect Effects 0.000 claims description 4
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- 239000013008 thixotropic agent Substances 0.000 claims description 3
- 239000003999 initiator Substances 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 22
- -1 methacryloyl Chemical group 0.000 description 16
- 229910052739 hydrogen Inorganic materials 0.000 description 14
- 239000001257 hydrogen Substances 0.000 description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 125000005395 methacrylic acid group Chemical group 0.000 description 3
- 230000008719 thickening Effects 0.000 description 3
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 239000012776 electronic material Substances 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 238000000016 photochemical curing Methods 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- DDKMFQGAZVMXQV-UHFFFAOYSA-N (3-chloro-2-hydroxypropyl) 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CCl DDKMFQGAZVMXQV-UHFFFAOYSA-N 0.000 description 1
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- NEBBLNDVSSWJLL-UHFFFAOYSA-N 2,3-bis(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(OC(=O)C(C)=C)COC(=O)C(C)=C NEBBLNDVSSWJLL-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JJBFVQSGPLGDNX-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)COC(=O)C(C)=C JJBFVQSGPLGDNX-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- RIYDSTPQZDWTBD-UHFFFAOYSA-N 2-[2-[2-[2-(2-chloroprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-chloroprop-2-enoate Chemical compound ClC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(Cl)=C RIYDSTPQZDWTBD-UHFFFAOYSA-N 0.000 description 1
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- UVJFHVAXZILJFX-UHFFFAOYSA-N 2-methylprop-2-enoic acid propane-1,2,3-triol Chemical compound CC(=C)C(O)=O.CC(=C)C(O)=O.CC(=C)C(O)=O.CC(=C)C(O)=O.OCC(O)CO UVJFHVAXZILJFX-UHFFFAOYSA-N 0.000 description 1
- SNKCYVQJXNSZCN-UHFFFAOYSA-N C(C(=C)C)(=O)OC1(C(C(C(C=C1)(C(C)(C)C1(C(C(C(C=C1)(OC(C(=C)C)=O)OCC)(OCC)OCC)(OCC)OCC)OCC)OCC)(OCC)OCC)(OCC)OCC)OCC Chemical compound C(C(=C)C)(=O)OC1(C(C(C(C=C1)(C(C)(C)C1(C(C(C(C=C1)(OC(C(=C)C)=O)OCC)(OCC)OCC)(OCC)OCC)OCC)OCC)(OCC)OCC)(OCC)OCC)OCC SNKCYVQJXNSZCN-UHFFFAOYSA-N 0.000 description 1
- IAQGBSCAEBIZOF-UHFFFAOYSA-N C(C(=C)C)(=O)OC1(C(C(C(CC1(OCC)OCC)(C(C)(C)C1(C(C(C(C(C1)(OCC)OCC)(OC(C(=C)C)=O)OCC)(OCC)OCC)(OCC)OCC)OCC)OCC)(OCC)OCC)(OCC)OCC)OCC Chemical compound C(C(=C)C)(=O)OC1(C(C(C(CC1(OCC)OCC)(C(C)(C)C1(C(C(C(C(C1)(OCC)OCC)(OC(C(=C)C)=O)OCC)(OCC)OCC)(OCC)OCC)OCC)OCC)(OCC)OCC)(OCC)OCC)OCC IAQGBSCAEBIZOF-UHFFFAOYSA-N 0.000 description 1
- FXNGCWSEOIEXLT-UHFFFAOYSA-N C(C(=C)C)(=O)OC1(C(C(C(CC1(OCCC)OCCC)(C(C)(C)C1(C(C(C(C(C1)(OCCC)OCCC)(OC(C(=C)C)=O)OCCC)(OCCC)OCCC)(OCCC)OCCC)OCCC)OCCC)(OCCC)OCCC)(OCCC)OCCC)OCCC Chemical compound C(C(=C)C)(=O)OC1(C(C(C(CC1(OCCC)OCCC)(C(C)(C)C1(C(C(C(C(C1)(OCCC)OCCC)(OC(C(=C)C)=O)OCCC)(OCCC)OCCC)(OCCC)OCCC)OCCC)OCCC)(OCCC)OCCC)(OCCC)OCCC)OCCC FXNGCWSEOIEXLT-UHFFFAOYSA-N 0.000 description 1
- TVINCDSDCBQPOU-UHFFFAOYSA-N C(C(=C)C)(=O)OC1(C(C(C(CC1(OCCCC)OCCCC)(C(C)(C)C1(C(C(C(C(C1)(OCCCC)OCCCC)(OC(C(=C)C)=O)OCCCC)(OCCCC)OCCCC)(OCCCC)OCCCC)OCCCC)OCCCC)(OCCCC)OCCCC)(OCCCC)OCCCC)OCCCC Chemical compound C(C(=C)C)(=O)OC1(C(C(C(CC1(OCCCC)OCCCC)(C(C)(C)C1(C(C(C(C(C1)(OCCCC)OCCCC)(OC(C(=C)C)=O)OCCCC)(OCCCC)OCCCC)(OCCCC)OCCCC)OCCCC)OCCCC)(OCCCC)OCCCC)(OCCCC)OCCCC)OCCCC TVINCDSDCBQPOU-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- RLLJPSFBAVVKAR-UHFFFAOYSA-N OC(=O)C=C.OC(=O)C=C.OCC(O)CO.OCC(O)CO Chemical compound OC(=O)C=C.OC(=O)C=C.OCC(O)CO.OCC(O)CO RLLJPSFBAVVKAR-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- IMBMQFHFGLJTIP-UHFFFAOYSA-N [1,2,4,5,5,6,6-heptaethoxy-4-[2-[1,3,4,5,5,6,6-heptaethoxy-4-(2-methylprop-2-enoyloxy)cyclohex-2-en-1-yl]propan-2-yl]cyclohex-2-en-1-yl] 2-methylprop-2-enoate Chemical compound C(C(=C)C)(=O)OC1(C(C(C(C=C1OCC)(C(C)(C)C1(C(C(C(C(=C1)OCC)(OC(C(=C)C)=O)OCC)(OCC)OCC)(OCC)OCC)OCC)OCC)(OCC)OCC)(OCC)OCC)OCC IMBMQFHFGLJTIP-UHFFFAOYSA-N 0.000 description 1
- VSXPEHGZLDNBNU-UHFFFAOYSA-N [2,3,5,6-tetraethoxy-4-[2-[2,3,5,6-tetraethoxy-4-(2-methylprop-2-enoyloxy)phenyl]propan-2-yl]phenyl] 2-methylprop-2-enoate Chemical compound CCOC1=C(OC(=O)C(C)=C)C(OCC)=C(OCC)C(C(C)(C)C=2C(=C(OCC)C(OC(=O)C(C)=C)=C(OCC)C=2OCC)OCC)=C1OCC VSXPEHGZLDNBNU-UHFFFAOYSA-N 0.000 description 1
- HQTNHJPKEJUJBF-UHFFFAOYSA-N [2,3,6-tributoxy-4-[2-[2,3,5-tributoxy-4-(2-methylprop-2-enoyloxy)phenyl]propan-2-yl]phenyl] 2-methylprop-2-enoate Chemical compound CCCCOC1=C(OC(=O)C(C)=C)C(OCCCC)=CC(C(C)(C)C=2C(=C(OCCCC)C(OC(=O)C(C)=C)=C(OCCCC)C=2)OCCCC)=C1OCCCC HQTNHJPKEJUJBF-UHFFFAOYSA-N 0.000 description 1
- ODCIWVCNUFIELT-UHFFFAOYSA-N [2,3,6-triethoxy-4-[2-[2,3,5-triethoxy-4-(2-methylprop-2-enoyloxy)phenyl]propan-2-yl]phenyl] 2-methylprop-2-enoate Chemical compound CCOC1=C(OC(=O)C(C)=C)C(OCC)=CC(C(C)(C)C=2C(=C(OCC)C(OC(=O)C(C)=C)=C(OCC)C=2)OCC)=C1OCC ODCIWVCNUFIELT-UHFFFAOYSA-N 0.000 description 1
- CVMSDYSTQLDHOA-UHFFFAOYSA-N [2,3-dibutoxy-4-[2-(2,3-dibutoxy-4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical compound CCCCOC1=C(OC(=O)C=C)C=CC(C(C)(C)C=2C(=C(OCCCC)C(OC(=O)C=C)=CC=2)OCCCC)=C1OCCCC CVMSDYSTQLDHOA-UHFFFAOYSA-N 0.000 description 1
- CFPKQOJSRXLMMK-UHFFFAOYSA-N [2,3-dibutoxy-4-[2-[2,3-dibutoxy-4-(2-methylprop-2-enoyloxy)phenyl]propan-2-yl]phenyl] 2-methylprop-2-enoate Chemical compound CCCCOC1=C(OC(=O)C(C)=C)C=CC(C(C)(C)C=2C(=C(OCCCC)C(OC(=O)C(C)=C)=CC=2)OCCCC)=C1OCCCC CFPKQOJSRXLMMK-UHFFFAOYSA-N 0.000 description 1
- VFDUKFNYDROHCI-UHFFFAOYSA-N [2,3-diethoxy-4-[2-[2,3,5-triethoxy-4-(2-methylprop-2-enoyloxy)phenyl]propan-2-yl]phenyl] 2-methylprop-2-enoate Chemical compound CCOC1=C(OC(=O)C(C)=C)C(OCC)=CC(C(C)(C)C=2C(=C(OCC)C(OC(=O)C(C)=C)=CC=2)OCC)=C1OCC VFDUKFNYDROHCI-UHFFFAOYSA-N 0.000 description 1
- QOTGETJBHLUZIP-UHFFFAOYSA-N [2,3-dipropoxy-4-[2-[2,3,5-triethoxy-4-(2-methylprop-2-enoyloxy)phenyl]propan-2-yl]phenyl] 2-methylprop-2-enoate Chemical compound CCCOC1=C(OC(=O)C(C)=C)C=CC(C(C)(C)C=2C(=C(OCC)C(OC(=O)C(C)=C)=C(OCC)C=2)OCC)=C1OCCC QOTGETJBHLUZIP-UHFFFAOYSA-N 0.000 description 1
- UUQJMSSFMULZHR-UHFFFAOYSA-N [4,5,5,6,6-pentaethoxy-4-[2-[1,5,5,6,6-pentaethoxy-4-(2-methylprop-2-enoyloxy)cyclohex-2-en-1-yl]propan-2-yl]cyclohex-2-en-1-yl] 2-methylprop-2-enoate Chemical compound C(C(=C)C)(=O)OC1C(C(C(C=C1)(C(C)(C)C1(C(C(C(C=C1)OC(C(=C)C)=O)(OCC)OCC)(OCC)OCC)OCC)OCC)(OCC)OCC)(OCC)OCC UUQJMSSFMULZHR-UHFFFAOYSA-N 0.000 description 1
- YSKCRYMJUCLQDG-UHFFFAOYSA-N [4-[2-(2,3-diethoxy-4-prop-2-enoyloxyphenyl)propan-2-yl]-2,3-diethoxyphenyl] prop-2-enoate Chemical compound CCOC1=C(OC(=O)C=C)C=CC(C(C)(C)C=2C(=C(OCC)C(OC(=O)C=C)=CC=2)OCC)=C1OCC YSKCRYMJUCLQDG-UHFFFAOYSA-N 0.000 description 1
- SJSXBTSSSQCODU-UHFFFAOYSA-N [4-[2-[2,3-diethoxy-4-(2-methylprop-2-enoyloxy)phenyl]propan-2-yl]-2,3-diethoxyphenyl] 2-methylprop-2-enoate Chemical compound CCOC1=C(OC(=O)C(C)=C)C=CC(C(C)(C)C=2C(=C(OCC)C(OC(=O)C(C)=C)=CC=2)OCC)=C1OCC SJSXBTSSSQCODU-UHFFFAOYSA-N 0.000 description 1
- OVBVURBQNDAVHM-UHFFFAOYSA-N [4-[2-[4-(2-methylprop-2-enoyloxy)-2,3,5-tripropoxyphenyl]propan-2-yl]-2,3,6-tripropoxyphenyl] 2-methylprop-2-enoate Chemical compound CCCOC1=C(OC(=O)C(C)=C)C(OCCC)=CC(C(C)(C)C=2C(=C(OCCC)C(OC(=O)C(C)=C)=C(OCCC)C=2)OCCC)=C1OCCC OVBVURBQNDAVHM-UHFFFAOYSA-N 0.000 description 1
- RRXMSCIBDRKLQO-UHFFFAOYSA-N [4-[2-[4-(2-methylprop-2-enoyloxy)-2,3-dipropoxyphenyl]propan-2-yl]-2,3-dipropoxyphenyl] 2-methylprop-2-enoate Chemical compound CCCOC1=C(OC(=O)C(C)=C)C=CC(C(C)(C)C=2C(=C(OCCC)C(OC(=O)C(C)=C)=CC=2)OCCC)=C1OCCC RRXMSCIBDRKLQO-UHFFFAOYSA-N 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Landscapes
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28428585A JPS62143909A (ja) | 1985-12-19 | 1985-12-19 | 光硬化型組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28428585A JPS62143909A (ja) | 1985-12-19 | 1985-12-19 | 光硬化型組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62143909A JPS62143909A (ja) | 1987-06-27 |
| JPH0476363B2 true JPH0476363B2 (de) | 1992-12-03 |
Family
ID=17676549
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP28428585A Granted JPS62143909A (ja) | 1985-12-19 | 1985-12-19 | 光硬化型組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62143909A (de) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57131214A (en) * | 1980-12-18 | 1982-08-14 | Gen Electric | Abrasion resistant ultraviolet ray curable coating composition and manufacture |
| JPS581756A (ja) * | 1981-06-01 | 1983-01-07 | ゼネラル・エレクトリツク・カンパニイ | Ｕｖ硬化性組成物、被覆物品およびその製法 |
| JPS5993773A (ja) * | 1982-11-19 | 1984-05-30 | Matsushita Electric Works Ltd | ビニルエステル接着剤 |
-
1985
- 1985-12-19 JP JP28428585A patent/JPS62143909A/ja active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57131214A (en) * | 1980-12-18 | 1982-08-14 | Gen Electric | Abrasion resistant ultraviolet ray curable coating composition and manufacture |
| JPS581756A (ja) * | 1981-06-01 | 1983-01-07 | ゼネラル・エレクトリツク・カンパニイ | Ｕｖ硬化性組成物、被覆物品およびその製法 |
| JPS5993773A (ja) * | 1982-11-19 | 1984-05-30 | Matsushita Electric Works Ltd | ビニルエステル接着剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62143909A (ja) | 1987-06-27 |
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